Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
21751 BAA01g15820 A01 7691178 C T synonymous_variant LOW c.324C>T|p.Arg108Arg S182
21752 BAA01g15820 A01 7691275 G A missense_variant MODERATE c.421G>A|p.Val141Ile S117
21753 BAA01g15830 A01 7691394 C T upstream_gene_variant MODIFIER c.-4784C>T| S167
21754 BAA01g15820 A01 7691640 G A synonymous_variant LOW c.618G>A|p.Arg206Arg S92
21755 BAA01g15830 A01 7691741 G A upstream_gene_variant MODIFIER c.-4437G>A| S162
21756 BAA01g15820 A01 7691899 G A missense_variant MODERATE c.793G>A|p.Val265Ile S306
S308
21757 BAA01g15830 A01 7692082 C T upstream_gene_variant MODIFIER c.-4096C>T| S151
S263
21758 BAA01g15830 A01 7692436 G A upstream_gene_variant MODIFIER c.-3742G>A| S287
21759 BAA01g15830 A01 7692496 C T upstream_gene_variant MODIFIER c.-3682C>T| S100
21760 BAA01g15830 A01 7692751 C T upstream_gene_variant MODIFIER c.-3427C>T| S36
21761 BAA01g15830 A01 7692771 C T upstream_gene_variant MODIFIER c.-3407C>T| S267
21762 BAA01g15830 A01 7692843 T C upstream_gene_variant MODIFIER c.-3335T>C| S305
21763 BAA01g15830 A01 7693394 C T upstream_gene_variant MODIFIER c.-2784C>T| S10
21764 BAA01g15830 A01 7694344 G A upstream_gene_variant MODIFIER c.-1834G>A| S201
21765 BAA01g15830 A01 7695306 G A upstream_gene_variant MODIFIER c.-872G>A| S308
21766 BAA01g15830 A01 7695336 G A upstream_gene_variant MODIFIER c.-842G>A| S174
21767 BAA01g15830 A01 7695729 G A upstream_gene_variant MODIFIER c.-449G>A| S245
21768 BAA01g15830 A01 7695773 G A upstream_gene_variant MODIFIER c.-405G>A| S122
21769 BAA01g15840 A01 7696609 C T upstream_gene_variant MODIFIER c.-4030C>T| S184
21770 BAA01g15840 A01 7696847 C T upstream_gene_variant MODIFIER c.-3792C>T| S61
21771 BAA01g15830 A01 7697513 G A missense_variant MODERATE c.632G>A|p.Arg211Lys S262
21772 BAA01g15830 A01 7698483 C T synonymous_variant LOW c.1222C>T|p.Leu408Leu S179
21773 BAA01g15830 A01 7698718 C T missense_variant MODERATE c.1457C>T|p.Pro486Leu S127
21774 BAA01g15840 A01 7699444 G A upstream_gene_variant MODIFIER c.-1195G>A| S229
21775 BAA01g15840 A01 7699455 G A upstream_gene_variant MODIFIER c.-1184G>A| S259